Canonical Allele Identifier: CA402940558

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106638G>C (hg19) ; chr19:g.1106639G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106639G>C , CM000681.2:g.1106639G>C	GRCh38
NC_000019.9:g.1106638G>C , CM000681.1:g.1106638G>C	GRCh37
NC_000019.8:g.1057638G>C	NCBI36
NG_050621.1:g.7714G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*67G>C	ENSP00000473614.3:n.*67G>C
ENST00000593032.6:c.641G>C	ENSP00000465828.4:p.Ter214Ser
ENST00000706713.1:c.*67G>C	ENSP00000516510.1:n.*67G>C
ENST00000706714.1:c.641G>C	ENSP00000516511.1:p.Ter214Ser
ENST00000706715.1:c.*67G>C	ENSP00000516512.1:n.*67G>C
ENST00000354171.13:c.*67G>C MANE Select	ENSP00000346103.7:n.*67G>C
ENST00000589115.6:c.*93G>C	ENSP00000466872.3:n.*93G>C
ENST00000354171.12:c.*67G>C	ENSP00000346103.7:n.*67G>C
ENST00000585480.1:c.361G>C	ENSP00000467900.1:p.Asp121His
ENST00000588919.5:c.602G>C	ENSP00000464989.3:p.Ter201Ser
ENST00000589115.5:c.*93G>C	ENSP00000466872.2:n.*93G>C
ENST00000592940.2:n.1032G>C
ENST00000611653.4:c.*67G>C	ENSP00000483655.1:n.*67G>C
ENST00000616066.4:c.*67G>C	ENSP00000485000.1:n.*67G>C
ENST00000622390.4:c.*67G>C	ENSP00000477503.1:n.*67G>C
NM_001039847.2:c.683G>C	NP_001034936.1:p.Ter228Ser
NM_001039848.2:c.*67G>C	NP_001034937.1:n.*67G>C
NM_002085.4:c.*67G>C	NP_002076.2:n.*67G>C
NM_001039848.3:c.*67G>C	NP_001034937.1:n.*67G>C
NM_001039847.3:c.683G>C	NP_001034936.1:p.Ter228Ser
NM_001039848.4:c.*67G>C	NP_001034937.1:n.*67G>C
NM_001367832.1:c.*67G>C	NP_001354761.1:n.*67G>C
NM_002085.5:c.*67G>C MANE Select	NP_002076.2:n.*67G>C